2026 data FDA MAUDE openFDA

Modular Electromechanical Surgical System

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

OpenFDA device adverse-event casebook.

FDA MAUDE casebook

openFDA event book Modular Electromechanical Surgical System LIGHT-BOOK · MAUDE

#947 of 1000 · 404 reports · 2025–2026

  • BOOK 404 reports
  • RANK #947 of 1000
  • DEATH 0 death-typed
  • INJ 6 injury-typed
  • MALF 398 malfunction
  • SPAN 2025–2026
  • PEAK 2026: 320
  • PHOTO Camera, Scintillation

Nearest event-volume peer: Camera, Scintillation (Gamma) (0 report gap)

Modular Electromechanical Surgical System sits #947 of 1000 among tracked device types with 404 MAUDE reports spanning 2025–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →

Event-type mix vs corpus

Shares of FDA event_type codes on this device type, compared with the mean across 1,000 device types that have ≥100 MAUDE reports. Codes are report labels, not adjudicated causation.

  • DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
  • INJ 1.5% corpus 30.4% · below corpus mean (-29.0 pp)
  • MALF 98.5% corpus 64.5% · above corpus mean (+34.0 pp)

Lead product-problem code Application Program Freezes, Becomes Nonfunctional is 15% of coded problems · Lead manufacturer DAVIS & GECK CARIBE LTD accounts for 75% of manufacturer-tagged reports · Top event location is 100% of location-tagged rows .

Modular Electromechanical Surgical System in the event-volume neighbourhood

FDA MAUDE report totals among this device type and nearest nationwide peers

reports

What this shows Modular Electromechanical Surgical System carries 404 MAUDE reports, ranked #947 of 1000.

Source FDA MAUDE via openFDA, aggregated by PlainHospital As of August 2026

Event Types

Malfunction 398 (98.5%)
Injury 6 (1.5%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

387 (96.3%)
R 4 (1.0%)
Other 4 (1.0%)
L 2 (0.5%)
O 2 (0.5%)
H 1 (0.2%)
Hospitalization 1 (0.2%)
Required Intervention 1 (0.2%)

Top Product Problems

Application Program Freezes, Becomes Nonfunctional 91
Intermittent Communication Failure 83
Break 72
Communication or Transmission Problem 72
Display or Visual Feedback Problem 52
Difficult to Remove 38
Difficult or Delayed Activation 34
Device Fell 28
Failure to Calibrate 26
Positioning Problem 16
Activation Problem 14
No Display/Image 13
Unintended Collision 10
Component or Accessory Incompatibility 9
Use of Device Problem 7
Connection Problem 6
No Apparent Adverse Event 6
Unintended System Motion 6
Device Displays Incorrect Message 5
Noise, Audible 5

Yearly Trend

25
2025: 84
26
2026: 320

Related Entities for Modular Electromechanical Surgical System

Event Locations

404 (100.0%)

Compare DAVIS & GECK CARIBE LTD vs COVIDIEN SURGICAL →

Nationwide devices with similar MAUDE profiles

Two openFDA-derived peer sets for Modular Electromechanical Surgical System, both floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (404 here).

Similar death-typed counts

Nearest other device types by death-typed report count (0 here), distinct from the volume row.

Disclaimer: MAUDE figures for Modular Electromechanical Surgical System are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.

Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Modular Electromechanical Surgical System; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.